|
HS Code |
429339 |
| Cas Number | 4114-31-2 |
| Iupac Name | 5-hydroxypyridine-2-carboxamide |
| Molecular Formula | C6H6N2O2 |
| Molecular Weight | 138.13 |
| Appearance | White to off-white solid |
| Melting Point | 225-230°C |
| Solubility In Water | Moderate |
| Boiling Point | Decomposes before boiling |
| Pubchem Cid | 31984 |
| Smiles | C1=CC(=NC=C1O)C(=O)N |
| Inchi | InChI=1S/C6H6N2O2/c7-6(10)5-3-4(9)1-2-8-5/h1-3,9H,(H2,7,10) |
| Storage Conditions | Store in a cool, dry place, protected from light and moisture |
As an accredited 5-Hydroxypyridine-2-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle labeled "5-Hydroxypyridine-2-carboxamide, 25g." Features hazard pictograms, lot number, CAS, purity, and supplier details. |
| Container Loading (20′ FCL) | 20′ FCL container holds 12MT of 5-Hydroxypyridine-2-carboxamide, packed in 25kg fiber drums, with inner polyethylene liners. |
| Shipping | 5-Hydroxypyridine-2-carboxamide is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be packaged according to standard regulations for laboratory chemicals, labeled appropriately, and accompanied by a Safety Data Sheet (SDS). The chemical is shipped at ambient temperature unless otherwise specified, ensuring safe transit and storage conditions. |
| Storage | **5-Hydroxypyridine-2-carboxamide** should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Store at room temperature and avoid exposure to heat or open flames. Ensure proper labeling and follow local safety guidelines for chemical storage. |
| Shelf Life | Shelf Life: 5-Hydroxypyridine-2-carboxamide is stable for at least 2 years when stored in a cool, dry place, protected from light. |
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Purity 99%: 5-Hydroxypyridine-2-carboxamide with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting Point 230°C: 5-Hydroxypyridine-2-carboxamide with melting point 230°C is used in high-temperature organic reactions, where it maintains structural integrity under thermal stress. Molecular Weight 138.12 g/mol: 5-Hydroxypyridine-2-carboxamide with molecular weight 138.12 g/mol is used in analytical standard preparation, where it provides precise calibration for mass spectrometry. Particle Size <50 µm: 5-Hydroxypyridine-2-carboxamide with particle size less than 50 micrometers is used in fine chemical formulations, where it facilitates uniform dispersion and rapid dissolution. Stability Temperature up to 180°C: 5-Hydroxypyridine-2-carboxamide with stability temperature up to 180°C is used in catalyst development, where it resists decomposition and extends catalyst lifespan. Solubility in Water 10 g/L: 5-Hydroxypyridine-2-carboxamide with solubility in water of 10 grams per liter is used in aqueous medicinal chemistry assays, where it allows for efficient bioavailability testing. Residual Solvent <0.1%: 5-Hydroxypyridine-2-carboxamide with residual solvent content less than 0.1% is used in active pharmaceutical ingredient manufacturing, where it meets stringent regulatory compliance for purity. UV Absorption λmax 275 nm: 5-Hydroxypyridine-2-carboxamide with UV absorption maximum at 275 nm is used in spectroscopic analysis, where it enables sensitive detection and quantification in quality control processes. |
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Most days in a lab, some compounds make an outsized impact without much fanfare. Among the unsung staples in chemical research, 5-Hydroxypyridine-2-carboxamide quietly delivers flexibility across several scientific fields. As someone who has tested plenty of pyridine derivatives on real experiments—not just in theory—I know how a pure sample can set the stage for a successful outcome. With its robust structure and reliable performance, this compound draws the attention of researchers who demand clarity at every step.
Let’s paint a clear picture: This molecule, identified by its formula C6H6N2O2, carries the strength of a pyridine ring substituted at the 2-position by a carboxamide group and at the 5-position by a hydroxyl group. This small twist in its structure opens different possibilities compared to plain pyridine or generic carboxamides. The white to off-white crystalline powder tends to attract the eye—pure compounds have a look and handle that seasoned chemists recognize. The melting point, solubility, and storage needs stand where you’d expect any research-grade compound to be, yet the subtle differences in reactivity and compatibility push 5-Hydroxypyridine-2-carboxamide into a niche all its own.
While newer materials flash onto the scene, this compound’s consistent chemistry keeps it a mainstay in organic synthesis, pharmaceutical exploration, and analytical reference. You won’t find it in every chemistry drawer, but the teams pushing into the next generation of reaction mechanisms or tweaking new drug leads reach for it frequently. It bridges the gap between classic laboratory staples and more specialized reagents—much like how simple boronic acids became almost legendary in coupling chemistry.
Molecular structure genuinely matters. The 5-hydroxyl group on this pyridine ring means hydrogen bonding can play a bigger role in solutions and solid states. That opens up unique opportunities for creating derivatives or intermediates that interact in ways you simply can’t get from unsubstituted pyridine or plain nicotinamide. Chemists looking to move beyond redundant conditions or dead-end reactions often find their curiosity piqued by the difference one functional group makes.
From a practical point of view, this structure means the compound dissolves with predictable results in polar solvents such as water, ethanol, or DMSO. When I’ve needed to coax reluctant reactants into a clean conversion, adding a compound with just the right solubility and reactivity makes all the difference. This is especially true when aiming for precision in small-scale syntheses or bioassays, where one wrong solvent or additive ends in frustration. Over time, I’ve realized that trusting the specifications of 5-Hydroxypyridine-2-carboxamide streamlines protocol optimization, saving both time and chemistry budget.
This compound emerges most often on the bench where innovation happens—always a sure sign of its actual value rather than marketing hype. Academic labs rely on it as a building block for synthesizing more involved molecules, often where hydrogen bonding plays a key part in biological testing. Its amide and hydroxyl groups lend themselves to selective modification, making it a springboard for analog synthesis. Years ago, I watched a colleague use it to generate a suite of new materials, each with a different substitution pattern. The ability to reliably transform the starting compound into custom targets raised the conversation from “What can we do?” to “How far can we go?”
Pharmaceutical teams appreciate this versatility. Drug discovery never stops searching for ways to introduce new patterns onto heterocycles, and the ready availability of 5-Hydroxypyridine-2-carboxamide means structure-activity relationship studies pick up speed. One project I supported involved screening new enzyme inhibitors, where subtle changes in the core molecule tipped the balance on activity. This compound gave us that flexibility without fighting downstream side reactions.
Testing in analytical chemistry also favors a rock-solid standard. Having reliable purity and a known melting point becomes essential for setting up chromatographic or spectroscopic protocols. That may not sound glamorous, but good data starts with confidence in your reference material. I have watched more than one new student learn this the hard way when a supposedly “fresh” sample led a column astray, sending the project back to square one. The more these basic hurdles are removed, the more you can trust the conclusions.
In a market crowded with similar molecules, it gets tempting to see all pyridine derivatives as interchangeable. In reality, minor structural differences dramatically impact how a compound feels to handle and behaves in the lab. Compared to 2-pyridinecarboxamide, 5-Hydroxypyridine-2-carboxamide brings an extra point of interaction, opening up new hydrogen bonds and electronic effects. Side by side, reactions diverge and product profiles shift. As many times as I’ve swapped in a new derivative hoping for a quick fix, the unique features of this molecule deliver distinct advantages—especially when other approaches fall flat.
Another common option is nicotinamide itself, serving as a vitamin B3 analogue. Yet the 5-hydroxyl version walks a fine line: adding adaptability for chemical synthesis and property tuning, without straying so far from the parent structure as to become unpredictable. This kind of balance rarely happens by coincidence—there’s a reason custom synthesis catalogs keep this item clearly marked. For seasoned researchers and newcomers alike, this predictable stretch of chemical space keeps it a go-to reagent for targeted experimentation.
Quality assurance in any chemical supply chain matters. Too many labs have lost time and resources due to mislabelled, contaminated, or subpar reagents. 5-Hydroxypyridine-2-carboxamide illustrates a case where the difference between high-grade and commodity material becomes crystal clear. I have seen batches from questionable sources that left behind mysterious residues on glassware—clouding NMR spectra, slowing purification, and turning routine workups into marathons of troubleshooting. Fortunately, suppliers focused on research markets tend to uphold higher standards: providing documented purity, batch analysis, and verified melting points. Sticking to these channels pays for itself by preventing setbacks down the line.
Certification and transparent supply chains help researchers avoid headaches. In my experience, the labs that skip these steps wind up with unreliable data, reproducibility nightmares, and looming deadlines. It’s easier to troubleshoot a reaction by checking solvent ratios or stoichiometry than to untangle what went wrong with an impure intermediate. That’s why clear communication between chemistry partners makes for lasting relationships—whether in academia or industry.
No one working with chemicals can ignore environmental responsibilities, and 5-Hydroxypyridine-2-carboxamide fits into the growing discussion around laboratory waste and green chemistry. While it’s not volatile or acutely toxic at small scales, its proper disposal and handling matter just as much as for larger classes of reagents. I’ve always preferred labs that educate their teams on waste protocols—segregating nitrogens, keeping carboxylic acids and amides separate, and minimizing unnecessary use.
Safe storage boils down to dry, cool, and clearly labeled containers. Every lab tech learns quickly how much hassle a poorly capped bottle or contaminated scoop can cause. Proper training, attention, and an investment in good personal protective equipment leave fewer excuses for lost or ruined batches. Responsible sourcing, smart usage, and efficient disposal all contribute to research that respects both human health and the broader environment.
As technology races ahead, 5-Hydroxypyridine-2-carboxamide maintains its role in the transition from routine synthesis to more targeted applications. Advances in medicinal chemistry hint at new uses, with more teams exploring fine-tuned signaling pathways, chelation, or even specialty polymer production. Its adaptable structure keeps it at the center of brainstorming sessions—researchers seeking more than just another plain heterocycle.
Recent publications highlight how small modifications of this molecule enable fluorescent labeling, new analytical probes, or subtle controls over molecular recognition. Rather than being locked into legacy chemistry, teams reimagine what’s possible, using reliable scaffolds for faster cycles of design, test, and refinement. The bridge between established practice and innovative thinking shows just how enduring certain compounds can be, especially when supported by sound research standards and shared best practices.
Every useful molecule brings its own set of hurdles. For 5-Hydroxypyridine-2-carboxamide, ensuring consistent supply and purity stands out. Smaller labs may struggle to access top-tier products at reasonable prices, and large-scale users must watch batch variability and delivery timing. Collective initiatives among universities and research consortia offer one approach—pooling orders, verifying suppliers, and establishing in-house quality checks.
Reproducibility remains key in research. Maintaining a consistent workflow—standardizing measurements, checking certificates of analysis, and preserving samples—makes the difference between a random result and a reliable series. For journal submissions, patent filings, or regulatory steps, traceable materials give substance to otherwise abstract claims.
Information-sharing can shift the whole field. Detailed reporting of reagent quality, solvent systems, and storage methods helps fellow scientists avoid pitfalls. Many accomplished teams dedicate part of their publications or supporting data to describing exactly which grade of 5-Hydroxypyridine-2-carboxamide worked, offering real-world guidance and reducing needless repetition.
Quality research starts with informed scientists. Training programs increasingly emphasize the importance of understanding both the capabilities and the quirks of compounds like 5-Hydroxypyridine-2-carboxamide. My own mentors insisted on triple-checking reagent specifications and batch numbers, which prevented so much wasted time on irreproducible outcomes. New researchers gain confidence when they recognize the telltale signs of a pure sample: sharp melting points, reliable NMR peaks, and clean TLC plates.
Organizational culture influences these habits. Labs that prioritize clear documentation, standardized protocols, and data integrity see better results and faster progress. Collaborative environments accelerate learning and innovation—the more a team knows about their materials, the more they achieve together.
The world’s appetite for new molecules never wanes, and demand for reliable reagents keeps evolving. Emerging fields such as precision medicine, green chemistry, and advanced materials science generate interest in compounds with unique reactivity or solubility profiles. The distinguishing features of 5-Hydroxypyridine-2-carboxamide make it a workhorse for targeted therapies, specialty polymers, and analytical methods pushing beyond conventional boundaries.
Accessibility remains a key challenge. Researchers in regions with limited infrastructure may have trouble sourcing high-quality compounds or consistent documentation. Digital supply chains and open-access protocols are starting to level the field, but there is more work to be done. When researchers make their findings accessible and transparent, the broader community benefits—paving the way for discoveries that no single team could achieve alone.
Science moves faster through collaboration, and shared use of key reagents supports a trust-based research culture. Suppliers who work closely with customers—solving shipping, purity, or technical support issues—help everyone stay focused on discovery. Groups that share best practices across institutions foster creative approaches, and open data sharing allows successes and failures alike to shape the next round of experimentation. During my career, conversations around the “right” material have solved countless roadblocks; often the difference comes down to one team's deeper knowledge of handling and troubleshooting.
Conferences, online forums, and collaborative grants enable these conversations. The value of firsthand experience cannot be overstated when it comes to optimizing a reaction or switching to a novel analog. Listening to a senior chemist describe the time they salvaged an entire screen by purging a questionable lot speaks more loudly than another training handout ever could.
Innovation depends on reliable foundations. Compounds like 5-Hydroxypyridine-2-carboxamide offer a stable platform for discovery and incremental improvement. The lessons learned from working with well-characterized materials extend beyond chemistry: they inspire attention to detail, rigorous record-keeping, and mutual support. Over time, these habits drive science forward in ways that simple novelty never could.
Looking back across years in the field, the compounds that researchers return to time and again share certain qualities: predictable handling, trustworthy specifications, and the flexibility to adapt to new challenges. Through countless experiments, failed runs, and unexpected breakthroughs, 5-Hydroxypyridine-2-carboxamide proves its worth not simply by being available, but by helping science ask better questions—and trust the answers that follow.
5-Hydroxypyridine-2-carboxamide may not carry a marketing buzz or headline-making profile. Yet, for those who prize steady, observable progress and meaningful experiments, it continues to earn its place on the shelf. From refining old methods to probing the next generation of scientific ideas, it stands out less by dramatic transformation and more by reliably enabling progress in the hands of those who know how to use it. As research standards evolve and expectations rise, a solid, well-understood compound never stops rewarding those who build with care and purpose.